“I’m not convinced.”
Those were the words out of my decade-long relationship with my trusted electrophysiologist. I saw her on and off for 10 years during the moments I had insurance. I had 4 cardiac ablations for supraventricular tachycardia (SVT) from a congenital heart disorder called Wolff-Parkinson-White Syndrome, which is an extra electrical conduction pathway between chambers that cause arrhythmias. My heart rates would go up to 300s and drop down to the 30s. No, that wasn’t a typo. After four cardiac ablations and still having arrhythmias and fast heart rates, I could not take meds to slow down my heart since my rate would drop low too. I spent years in that position… in limbo without treatment and a chaotic heart.
My valves began to deteriorate as well, causing even more issues. I had open heart surgery for an aortic valve repair in 2011 and will need a replacement in the future, requiring open heart surgery again.
My trusted doctor, told me that it sounded like I was dealing with something that was too rare and not likely possible. She wasn’t convinced I could have another rare disorder. She denied me treatment. I was afraid to sleep at night, afraid that I wouldn’t wake up. Did you know you can pass out in your sleep? I finally collected my most recent 50 page heart event monitor report from the VP of the device company (my doctor would not give me the reports) and took it to another doctor. He ordered a Tilt Table Test and induced an episode and found that I had a severe cardioinhibitory response and confirmed that I needed a pacemaker, wondering why it took so long.
Two weeks later, my life changed. My heart rate doesn’t pause, stop or plummet and I can take meds to keep my heart rate from going too high. The pacemaker even kicks in to reduce arrhythmias.
The puzzle pieces all came together after seeing specialists and understanding why I was having a dysfunctional nervous system and irregular heart, chronic pain, chronic fatigue and an array of health issues. Genetic testing, research and being my own advocate helped more than anything. It took my entire life to get answers. I learned that I have Ehlers-Danlos Syndrome, a connective tissue disorder that causes many of my health issues on top of WPW Syndrome. Having WPW made is harder to see that something more could be going on because everyone was focused on that.
I never want anyone else to ever have to go through what I have gone through. I never want anyone else to be medically neglected, dismissed or too rare for their doctor to be convinced. There is an entire world of people suffering in the dark. My mission is to change that. I raise awareness for those people that feel alone, lost and ignored while they fear for their lives, praying to wake up the next morning.